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BROVIAC SINGLE LUMEN CV CATHETER CUTDOWN TRAY WITH SURECUFF TISSUER INGROWTH CUFF - FDA Registration MDR-07615

Access comprehensive regulatory information for BROVIAC SINGLE LUMEN CV CATHETER CUTDOWN TRAY WITH SURECUFF TISSUER INGROWTH CUFF in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07615 and manufactured by Bard Access Systems, Inc. in Mexico. The device was registered on April 29, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Rebmann Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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MDR-07615
BROVIAC SINGLE LUMEN CV CATHETER CUTDOWN TRAY WITH SURECUFF TISSUER INGROWTH CUFF
Registered medical device in Philippines
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Device Information
Product Name
BROVIAC SINGLE LUMEN CV CATHETER CUTDOWN TRAY WITH SURECUFF TISSUER INGROWTH CUFF
Registration Number
MDR-07615
Manufacturer Details
Country of Origin
Mexico
Importer & Distribution
Importer/Distributor
Rebmann Inc.
Registration Dates
Issuance Date
April 29, 2020
Expiry Date
December 19, 2024